High-Performance Biodegradable Energy Storage Devices Enabled by Heterostructured MoO3–MoS2 Composites

Biodegradable implantable devices are of growing interest in biosensors and bioelectronics. One of the key unresolved challenges is the availability of power supply. To enable biodegradable energy-storage devices, herein, 2D heterostructured MoO₃–MoS₂ nanosheet arrays are synthesized on water-soluble Mo foil, showing a high areal capacitance of 164.38 mF cm⁻² (at 0.5 mA cm⁻²). Employing the MoO₃–MoS₂ composite as electrodes of a symmetric supercapacitor, an asymmetric Zn-ion hybrid supercapacitor, and an Mg primary battery are demonstrated. Benefiting from the advantages of MoO₃–MoS₂ heterostructure, the Zn-ion hybrid supercapacitors deliver a high areal capacitance (181.86 mF cm⁻² at 0.5 mA cm⁻²) and energy density (30.56 µWh cm⁻²), and the Mg primary batteries provide a stable high output voltage (≈1.6 V) and a long working life in air/liquid environment. All of the used materials exhibit desirable biocompatibility, and these fabricated devices are also fully biodegradable. Demonstration experiments display their potential applications as biodegradable power sources for various electronic devices.     

Hydroxyapatite-Derived Heterogeneous Ru-Ru2P Electrocatalyst and Environmentally-Friendly Membrane Electrode toward Efficient Alkaline Electrolyzer

Alkaline membrane water electrolysis is a promising production technology, and advanced electrocatalyst and membrane electrode design have always been the core technology. Herein, an ion-exchange method and an environmentally friendly in situ green phosphating strategy are successively employed to fabricate Ru-Ru₂P heterogeneous nanoparticles by using hydroxyapatite (HAP) as a phosphorus source, which is an exceptionally active electrocatalyst for hydrogen evolution reaction (HER). Density functional theory calculation results reveal that strong electronic redistribution occurs at the heterointerface of Ru-Ru₂P, which modulates the electronic structure to achieve an optimized hydrogen adsorption strength. The obtained Ru-Ru₂P possesses excellent HER performance (24 mV at 10 mA cm⁻²) and robust stability (1000 mA cm⁻² for 120 h) in alkaline media. Furthermore, an environmentally friendly membrane electrode with a sandwich structure is assembled by HAP nanowires as an alkaline membrane, Ru-Ru₂P as a cathodic catalyst, and NiFe-LDH as an anodic catalyst, respectively. The voltage of (−) Ru-Ru₂P || NiFe-LDH/CNTs (+) (1.53 V at 10 mA cm⁻²) is lower than that of (−) 20 wt% Pt/C || RuO₂ (+) (1.60 V at 10 mA cm⁻²) for overall water splitting. Overall, the studies not only design an efficient catalyst but also provide a new route to achieve a high-stability electrolyzer for industrial H₂ production.     

3D-Printed Structure Boosts the Kinetics and Intrinsic Capacitance of Pseudocapacitive Graphene Aerogels

The performance of pseudocapacitive electrodes at fast charging rates are typically limited by the slow kinetics of Faradaic reactions and sluggish ion diffusion in the bulk structure. This is particularly problematic for thick electrodes and electrodes highly loaded with active materials. Here, a surface-functionalized 3D-printed graphene aerogel (SF-3D GA) is presented that achieves not only a benchmark areal capacitance of 2195 mF cm⁻² at a high current density of 100 mA cm⁻² but also an ultrahigh intrinsic capacitance of 309.1 µF cm⁻² even at a high mass loading of 12.8 mg cm⁻². Importantly, the kinetic analysis reveals that the capacitance of SF-3D GA electrode is primarily (93.3%) contributed from fast kinetic processes. This is because the 3D-printed electrode has an open structure that ensures excellent coverage of functional groups on carbon surface and facilitates the ion accessibility of these surface functional groups even at high current densities and large mass loading/electrode thickness. An asymmetric device assembled with SF-3D GA as anode and 3D-printed GA decorated with MnO₂ as cathode achieves a remarkable energy density of 0.65 mWh cm⁻² at an ultrahigh power density of 164.5 mW cm⁻², outperforming carbon-based supercapacitors operated at the same power density.     

Design of Novel Wearable,Stretchable, and Waterproof Cable‐Type Supercapacitors Based on High‐Performance Nickel Cobalt Sulfide‐Coated Etching‐Annealed Yarn Electrodes

Rapid advances in functional electronics bring tremendous demands on innovation toward effective designs of device structures. Yarn supercapacitors (SCs) show advantages of flexibility, knittability, and small size, and can be integrated into various electronic devices with low cost and high efficiency for energy storage. In this work, functionalized stainless steel yarns are developed to support active materials of positive and negative electrodes, which not only enhance capacitance of both electrodes but can also be designed into stretchable configurations. The as‐made asymmetric yarn SCs show a high energy density of 0.0487 mWh cm^?2 (10.19 mWh cm^?3) at a power density of 0.553 mW cm^?2 (129.1 mW cm^?3) and a specific capacitance of 127.2 mF cm^?2 under an operating voltage window of 1.7 V. The fabricated SC is then made into a stretchable configuration by a prestraining‐then‐releasing approach using polydimethylsiloxane (PDMS) tube, and its electrochemical performance can be well maintained when stretching up to a high strain of 100%. Moreover, the stretchable cable‐type SCs are stably workable under water‐immersed condition. The method opens up new ways for fabricating flexible, stretchable, and waterproof devices.     

Ultralight Flexible Electrodes of Nitrogen-Doped Carbon Macrotube Sponges for High-Performance Supercapacitors

Light-weight and flexible supercapacitors with outstanding electrochemical performances are strongly desired in portable and wearable electronics. Here, ultralight nitrogen-doped carbon macrotube (N-CMT) sponges with 3D interconnected macroporous structures are fabricated and used as substrate to grow nickel ferrite (NiFe₂O₄) nanoparticles by vapor diffusion–precipitation and in situ growth. This process effectively suppresses the agglomeration of NiFe₂O₄, enabling good interfacial contact between N-CMT sponges and NiFe₂O₄. More remarkably, the as-synthesized NiFe₂O₄/N-CMT composite sponges can be directly used as electrodes without additional processing that could cause agglomeration and reduction of active sites. Benefiting from the tubular structure and the synergetic effect of NiFe₂O₄ and N-CMT, the NiFe₂O₄/N-CMT-2 exhibits a high specific capacitance of 715.4 F g⁻¹ at a current density of 1 A g⁻¹, and 508.3 F g⁻¹ at 10 A g⁻¹, with 90.9% of capacitance retention after 50 000 cycles at 1 A g⁻¹ in an alkaline electrolyte. Furthermore, flexible supercapacitors are fabricated, yielding areal specific capacitances of 1397.4 and 1041.2 mF cm⁻² at 0.5 and 8 mA cm⁻², respectively. They also exhibit exceptional cycling performance with capacitance retention of 92.9% at 1 mA cm⁻² after 10 000 cycles under bending. This work paves a new way to develop flexible, light-weight, and high-performance energy storage devices.     

Ce Site in Amorphous Iron Oxyhydroxide Nanosheet toward Enhanced Electrochemical Water Oxidation

Iron oxyhydroxide has been considered an auspicious electrocatalyst for the oxygen evolution reaction (OER) in alkaline water electrolysis due to its suitable electronic structure and abundant reserves. However, Fe-based materials seriously suffer from the tradeoff between activity and stability at a high current density above 100 mA cm⁻². In this work, the Ce atom is introduced into the amorphous iron oxyhydroxide (i.e., CeFeO_xH_y) nanosheet to simultaneously improve the intrinsic electrocatalytic activity and stability for OER through regulating the redox property of iron oxyhydroxide. In particular, the Ce substitution leads to the distorted octahedral crystal structure of CeFeO_xH_y, along with a regulated coordination site. The CeFeO_xH_y electrode exhibits a low overpotential of 250 mV at 100 mA cm⁻² with a small Tafel slope of 35.1 mVdec⁻¹. Moreover, the CeFeO_xH_y electrode can continuously work for 300 h at 100 mA cm⁻². When applying the CeFeO_xH_y nanosheet electrode as the anode and coupling it with the platinum mesh cathode, the cell voltage for overall water splitting can be lowered to 1.47 V at 10 mA cm⁻². This work offers a design strategy for highly active, low-cost, and durable material through interfacing high valent metals with earth-abundant oxides/hydroxides.     

Revealing the Enhanced Thermoelectric Properties of Controllably Doped Donor-Acceptor Copolymer: The Impact of Regioregularity

Albeit considerable attention to the fast-developing organic thermoelectric (OTE) materials due to their flexibility and non-toxic features, it is still challenging to design an OTE polymer with superior thermoelectric properties. In this work, two “isomorphic” donor–acceptor (D–A) conjugated polymers are studied as the semiconductor in OTE devices, revealing for the first time the internal mechanism of regioregularity on thermoelectric performances in D–A type polymers. A higher molecular structure regularity can lead to higher crystalline order and mobility, higher doping efficiency, order of energy state, and thermoelectric (TE) performance. As a result, the regioregular P2F exhibits a maximum power factor (PF) of up to 113.27 µW m⁻¹ K⁻², more than three times that of the regiorandom PRF (35.35 µW m⁻¹ K⁻²). However, the regular backbone also implies lower miscibility with a dopant, negatively affecting TE performance. Therefore, the trade-off between doping efficiency and miscibility plays a vital role in OTE materials, and this work sheds light on the molecular design strategy of OTE polymers with state-of-the-art performances.     

Self‐Supporting GaN Nanowires/Graphite Paper: Novel High‐Performance Flexible Supercapacitor Electrodes

Flexible supercapacitors have attracted great interest as energy storage devices because of their promise in applications such as wearable and smart electronic devices. Herein, a novel flexible supercapacitor electrode based on gallium nitride nanowire (GaN NW)/graphite paper (GP) nanocomposites is reported. The outstanding electrical conductivities of the GaN NW (6.36 × 10² S m^?1) and GP (7.5 × 10⁴ S m^?1) deliver a synergistically enhanced electrochemical performance that cannot be achieved by either of the components alone. The composite electrode exhibits excellent specific capacitance (237 mF cm^?2 at 0.1 mA cm^?2) and outstanding cycling performance (98% capacitance retention after 10 000 cycles). The flexible symmetric supercapacitor also manifests high energy and power densities (0.30 mW h cm^?3 and 1000 mW cm^?3). These findings demonstrate that the GaN/GP composite electrode has significant potential as a candidate for the flexible energy storage devices.     

Uniform Zinc Deposition Regulated by a Nitrogen-Doped MXene Artificial Solid Electrolyte Interlayer

The dendrite growth and side reactions of zinc metal anode in mildly acidic electrolytes seriously hinder the practical application of aqueous zinc–ion battery. To address these issues, an artificial protective layer of nitrogen-doped MXene (NMX) is used to protect the zinc anode. The NMX protective layer has high conductivity and uniformly distributed zincophilic sites, which can not only homogenize the local electric field on the electrode interface but also accelerate the kinetics for Zn deposition. As a result, the NMX protective layer induces uniform zinc deposition and reduces the overpotential of the electrode. Encouragingly, this NMX-protected Zn anode can cycle stably for 1900 h at 1 mA cm⁻² and 1 mAh cm⁻². In asymmetric cells, it achieves high cycle reversibility with an average Coulomb efficiency of 99.79% for 4800 cycles at 5 mA cm⁻².     

Exploring The Synergistic Effect Of CoSeP/CoP Interface Catalyst For Efficient Urea Electrolysis

Electrocatalytic oxidation of urea (UOR) is a potential energy-saving hydrogen production technology that can replace oxygen evolution reaction (OER). Therefore, CoSeP/CoP interface catalyst is synthesized on nickel foam using hydrothermal, solvothermal, and in situ template methods. The strong interaction of tailored CoSeP/CoP interface promotes the hydrogen production performance of electrolytic urea. During the hydrogen evolution reaction (HER), the overpotential can reach 33.7 mV at 10 mA cm⁻². The cell voltage can reach 1.36 V at 10 mA cm⁻² in the overall urea electrolytic process. Notably, the overall urine electrolysis performance of the catalyst in the human urine medium can reach 1.40 V at 10 mA cm⁻² and can exhibit durable cycle stability at 100 mA cm⁻². Density functional theory (DFT) proves that the CoSeP/CoP interface catalyst can better adsorb and stabilize reaction intermediates CO* and NH* on its surface through a strong synergistic effect, thus enhancing the catalytic activity.     

Accelerated Oxygen Evolution Kinetics by Engineering Heterojunction Coupling of Amorphous NiFe Hydr(oxy)oxide Nanosheet Arrays on Self-Supporting Ni-MOFs

Designing definite transition metal heterointerfaces is considered an effective strategy for the construction of efficient and robust oxygen evolution reaction (OER) electrocatalysts, but rather challenging. Herein, amorphous NiFe hydr(oxy)oxide nanosheet arrays (A-NiFe HNSAs) are grown in situ on the surface of a self-supporting Ni metal–organic frameworks (SNMs) electrode via a combination strategy of ion exchange and hydrolytic co-deposition for efficient and stable large-current-density water oxidation. The existence of the abundant metal–oxygen bonds on the heterointerfaces can not only be of great significance to alter the electronic structure and accelerate the reaction kinetics, but also enable the redistribution of Ni/Fe charge density to effectively control the adsorption behavior of important intermediates with a close to the optimal d-band center, dramatically narrowing the energy barriers of the OER rate-limiting steps. By optimizing the electrode structure, the A-NiFe HNSAs/SNMs-NF exhibits outstanding OER performance with small overpotentials of 223 and 251 mV at 100 and 500 mA cm⁻², a low Tafel slope of 36.3 mV dec⁻¹, and excellent durability during 120 h at 10 mA cm⁻². This work significantly provides an avenue to understand and realize rationally designed heterointerface structures toward effective oxygen evolution in water-splitting applications.     

Additive-Free Aqueous MXene Inks for Thermal Inkjet Printing on Textiles

Direct printing of functional inks onto flexible substrates allows for scalable fabrication of wearable electronics. However, existing ink formulations for inkjet printing require toxic solvents and additives, which make device fabrication more complex, limit substrate compatibility, and hinder device performance. Even water-based carbon or metal nanoparticle inks require supplemental surfactants, binders, and cosolvents to produce jettable colloidal suspensions. Here, a general approach is demonstrated for formulating conductive inkjet printable, additive-free aqueous Ti₃C₂T_x MXene inks for direct printing on various substrates. The rheological properties of the MXene inks are tuned by controlling the Ti₃C₂T_x flake size and concentration. Ti₃C₂T_x-based electrical conduits and microsupercapacitors (MSCs) are printed on textile and paper substrates by optimizing the nozzle geometry for high-resolution inkjet printing. The chemical stability and electrical properties of the printed devices are also studied after storing the devices for six months under ambient conditions. Current collector-free, textile-based MSCs show areal capacitance values up to 294 mF cm⁻² (2 mV s⁻¹) in poly(vinyl alcohol)/sulfuric acid gel electrolyte, surpassing reported printed MXene-based MSCs and inkjet-printed MSCs using other 2D nanomaterials. This work is an important step toward increasing the functional capacity of conductive inks and simplifying the fabrication of wearable textile-based electronics.     

3D Interdigital Au/MnO2/Au Stacked Hybrid Electrodes for On‐Chip Microsupercapacitors

On‐chip microsupercapacitors (MSCs) have application in powering microelectronic devices. Most of previous MSCs are made from carbon materials, which have high power but low energy density. In this work, 3D interdigital Au/MnO₂/Au stacked MSCs have been fabricated based on laser printed flexible templates. This vertical‐stacked electrode configuration can effectively increase the contact area between MnO₂ active layer and Au conductive layer, and thus improve the electron transport and electrolyte ion diffusion, resulting in enhanced pseudocapacitive performance of MnO₂. The stacked electrode can achieve an areal capacitance up to 11.9 mF cm^?2. Flexible and all‐solid‐state MSCs are assembled based on the sandwich hybrid electrodes and PVA/LiClO₄ gel electrolyte and show outstanding high‐rate capacity and mechanical flexibility. The laser printing technique in this work combined with the physical sputtering and electrodeposition allows fabrication of MSC array with random sizes and patterns, making them promising power sources for small‐scale flexible microelectronic energy storage systems (e.g., next‐generation smart phones).     

Dendrite-Free Potassium Metal Anodes in a Carbonate Electrolyte

Potassium (K) metal anodes suffer from a challenging problem of dendrite growth. Here, it is demonstrated that a tailored current collector will stabilize the metal plating–stripping behavior even with a conventional KPF₆-carbonate electrolyte. A 3D copper current collector is functionalized with partially reduced graphene oxide to create a potassiophilic surface, the electrode being denoted as rGO@3D-Cu. Potassiophilic versus potassiophobic experiments demonstrate that molten K fully wets rGO@3D-Cu after 6 s, but does not wet unfunctionalized 3D-Cu. Electrochemically, a unique synergy is achieved that is driven by interfacial tension and geometry: the adherent rGO underlayer promotes 2D layer-by-layer (Frank–van der Merwe) metal film growth at early stages of plating, while the tortuous 3D-Cu electrode reduces the current density and geometrically frustrates dendrites. The rGO@3D-Cu symmetric cells and half-cells achieve state-of-the-art plating and stripping performance. The symmetric rGO@3D-Cu cells exhibit stable cycling at 0.1–2 mA cm⁻², while baseline Cu prematurely fails when the current reaches 0.5 mA cm⁻². The half-cells cells of rGO@3D-Cu (no K reservoir) are stable at 0.5 mA cm⁻² for 10 000 min (100 cycles), and at 1 mA cm⁻² for 5000 min. The baseline 3D-Cu, planar rGO@Cu, and planar Cu foil fails after 5110, 3012, and 1410 min, respectively.     

Synergistic Solar-Driven Freshwater Generation and Electricity Output Empowered by Wafer-Scale Nanostructured Silicon

Electricity generation triggered by the ubiquitous water evaporation process provides an intriguing way to harvest energy from water. Meanwhile, natural water evaporation is also a fundamental way to obtain fresh water for human beings. Here, a wafer-scale nanostructured silicon-based device that takes advantage of its well-aligned configuration that simultaneously realizes solar steam generation (SSG) for freshwater collection and hydrovoltaic effect generation for electricity output is developed. An ingenious porous, black carbon nanotube fabric (CNF) electrode endows the device with sustainable water self-pumping capability, excellent durable conductivity, and intense solar spectrum harvesting. A combined device based on the CNF electrode integrated with nanostructured silicon nanowire arrays (SiNWs) provided an aligned numerous surface-to-volume water evaporation interface that enables a recorded continuous short-circuit current 8.65 mA and a water evaporation rate of 1.31 kg m⁻² h⁻¹ under one sun illumination. Such wafer-scale SiNWs-based SSG and hydrovoltaic integration devices would unchain the bottleneck of the weak and discontinuous electrical output of hydrovoltaic devices, which inspires other sorts of semiconductor-based hydrovoltaic device designs to target superior performance.     

A High-Energy Asymmetric Supercapacitor Based on Tomato-Leaf-Derived Hierarchical Porous Activated Carbon and Electrochemically Deposited Polyaniline Electrodes for Battery-Free Heart-Pulse-Rate Monitoring

A simple and scalable method to fabricate a novel high-energy asymmetric supercapacitor using tomato-leaf-derived hierarchical porous activated carbon (TAC) and electrochemically deposited polyaniline (PANI) for a battery-free heart-pulse-rate monitor is reported. In this study, TAC is prepared by simple pyrolysis, exhibiting nanosheet-type morphology and a high specific surface area of ≈1440 m² g⁻¹, and PANI is electrochemically deposited onto carbon cloth. The TAC- and PANI- based asymmetric supercapacitor demonstrates an electrochemical performance superior to that of symmetric supercapacitors, delivering a high specific capacitance of 248 mF cm⁻² at a current density of 1.0 mA cm⁻². The developed asymmetric supercapacitor shows a high energy density of 270 µWh cm⁻² at a power density of 1400 µW cm⁻², as well as an excellent cyclic stability of ≈95% capacitance retention after 10 000 charging–discharging cycles while maintaining ≈98% Coulombic efficiency. Impressively, the series-connected asymmetric supercapacitors can operate a battery-free heart-pulse-rate monitor extremely efficiently upon solar-panel charging under regular laboratory illumination.     

High Efficiency Near-Infrared Perovskite Light Emitting Diodes With Reduced Rolling-Off by Surface Post-Treatment

The rolling-off phenomenon of device efficiency at high current density caused by quenching of luminescence in perovskite light-emitting diodes (PeLED) is challenging to be solved. Here, 2-amino-5-iodopyrazine (AIPZ) is dissolved in a mixed solvent of chlorobenzene (CB)/isopropanol (IPA) (7:3 volume ratio) for surface post-treatment of FAPbI₃ perovskite film. The interaction of AIPZ and perovskite surface not only balances the charge injection but also passivates defects to enhance radiative recombination in PeLED. Therefore, the PeLED champion yields peak external quantum efficiency reaching 23.2% at the current density of 45 mA cm⁻² with a radiance brightness of 290 W sr⁻¹ m⁻². More importantly, the rolling-off of device efficiency is significantly reduced. The lowest rolling-off devices can maintain 80% of peak EQE (22.1%) at a high current density of 460 mA cm⁻², whereas the control device only retains 25% of the peak EQE value. This work provides an effective strategy to improve performance and reduce the EQE rolling-off of PeLED for practical application.     

Bimetallic Phosphide Heterostructure Coupled with Ultrathin Carbon Layer Boosting Overall Alkaline Water and Seawater Splitting

Seawater electrolysis is promising for green hydrogen production but hindered by the sluggish reaction kinetics of both cathode and anode, as well as the detrimental chlorine chemistry environment. Herein, a self-supported bimetallic phosphide heterostructure electrode strongly coupled with an ultrathin carbon layer on Fe foam (C@CoP-FeP/FF) is constructed. When used as an electrode for the hydrogen and oxygen evolution reactions (HER/OER) in simulated seawater, the C@CoP-FeP/FF electrode shows overpotentials of 192 mV and 297 mV at 100 mA cm⁻², respectively. Moreover, the C@CoP-FeP/FF electrode enables the overall simulated seawater splitting at the cell voltage of 1.73 V to achieve 100 mA cm⁻², and operate stably during 100 h. The superior overall water and seawater splitting properties can be ascribed to the integrated architecture of CoP-FeP heterostructure, strongly coupled carbon protective layer, and self-supported porous current collector. The unique composites can not only provide enriched active sites, ensure prominent intrinsic activity, but also accelerate the electron transfer and mass diffusion. This work confirms the feasibility of an integration strategy for the manufacturing of a promising bifunctional electrode for water and seawater splitting.     

Ultrastretchable MXene Microsupercapacitors

Stretchable microsupercapacitors represent emerging miniaturized energy-storage devices for next-generation deformable electronics. Two-dimensional (2D) transition metal carbides (MXenes) are considered attractive electrode materials due to their metallic conductivity, hydrophilic surfaces, and excellent processability. Here, an ultrastretchable microsupercapacitor of interdigitated MXene microelectrodes with crumpled surface textures is created. The microsupercapacitor shows a series of attractive properties including a high specific capacitance of ≈185 mF cm⁻², ultrahigh stretchability up to 800% area strain, and ≈89.7% retention of the initial capacitance after 1000 stretch–relaxation cycles. In addition to static strains, the microsupercapacitor demonstrates robust mechanical properties to retain stable charging–discharging capability under dynamic stretching at different strain rates. A self-powering circuit system utilizes four microsupercapacitor packs to power a light-emitting diode (LED) array, which exhibits stable operations under large tensile strain and skin-attached wearable settings. The developments offer a generic design strategy to enhance the deformability of microsupercapacitors based on 2D nanomaterials.     

Matching CP@NCOH/NF Cathode and GH/FNP/NF Anode for High-Performance Asymmetric Supercapacitor

It is extremely crucial to design and match high-quality cathode and anode for achieving high-performance asymmetric supercapacitors (ASCs). Herein, Co₃(PO₄)₂@NiCo-LDH/Ni foam (CP@NCOH/NF) cathode with hierarchical morphology and graphene hydrogel/Fe–Ni phosphide/Ni foam (GH/FNP/NF) anode with the robust and porous structure are elaborately designed and prepared, respectively. Owing to their unique and profitable structures, both CP@NCOH/NF and GH/FNP/NF electrodes yield the superior capacity (10760 and 2236 mC cm⁻² at 2 mA cm⁻², respectively), good rate capability (63% retention at 200 mA cm⁻² and 52% retention at 50 mA cm⁻², respectively), and excellent cycling stability (72% and 74% retention after 10 000 cycles, respectively). Benefiting from their matchable electrochemical performances, the configured solid-state CP@NCOH/NF//GH/FNP/NF ASC outputs both competitive energy density (80.2 Wh kg⁻¹/4.1 mWh cm⁻³) and power density (14563 W kg⁻¹/750 mW cm⁻³), companied by remarkable cyclability (71% retention after 10 000 cycles), manifesting its great promise for large-scale integrated energy-storage system.